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Identification of species of viridans group streptococci in clinical blood culture isolates by sequence analysis of the RNase P RNA gene, rnpB
被引:21
|作者:
Westling, Katarina
[1
]
Julander, Inger
[2
]
Ljungman, Per
[3
]
Vondracek, Martin
[4
]
Wretlind, Bengt
[5
]
Jalal, Shah
[5
]
机构:
[1] Karolinska Univ Hosp Huddinge, Dept Med, Div Infect Dis, Karolinska Inst, SE-14186 Stockholm, Sweden
[2] Karolinska Univ Hosp Solna, Dept Med, Div Infect Dis, SE-17176 Stockholm, Sweden
[3] Karolinska Univ Hosp Huddinge, Div Hematol, Dept Med, SE-14186 Stockholm, Sweden
[4] Karolinska Univ Hosp Solna, Dept Clin Microbiol Tumor & Cell Biol, Karolinska Inst, SE-17176 Stockholm, Sweden
[5] Karolinska Univ Hosp, Div Clin Bacteriol, Dept Lab Med, SE-14186 Stockholm, Sweden
关键词:
viridans group;
streptococci;
species identification;
infective endocarditis;
septicaemia;
molecular biological diagnostic methods;
RNase P RNA gene;
rnpB;
D O I:
10.1016/j.jinf.2007.12.006
中图分类号:
R51 [传染病];
学科分类号:
100401 ;
摘要:
Objectives: Viridans group streptococci (VGS) cause severe diseases such as infective endocarditis and septicaemia. Genetically, VGS species are very close to each other and it is difficult to identify them to species level with conventional methods. The aims of the present study were to use sequence analysis of the RNase P RNA gene (rnpB) to identify VGS species in clinical blood culture isolates, and to compare the results with the API 20 Strep system that is based on phenotypical characteristics. Methods: Strains from patients with septicaemia or endocarditis were analysed with PCR amplification and sequence analysis of the rnpB gene. Clinical data were registered as welt. Results: One hundred and thirty two VGS clinical blood culture isolates from patients with septicaemia (n = 95) or infective endocarditis (n = 36) were analysed; all but one were identified by rnpB. Streptococcus oralis, Streptococcus sanguinis and Streptococcus gordonii strains were most common in the patients with infective endocarditis. In the isolates from patients with haematological diseases, Streptococcus mitis and S. oralis dominated. In addition in 76 of the isolates it was possible to compare the results from rnpB analysis and the API 20 Strep system. In 39/76 (51%) of the isolates the results were concordant to species Level; in 55 isolates there were no results from API 20 Strep. Conclusion: Sequence analysis of the RNase P RNA gene (rnpB) showed that almost all isolates could be identified. This could be of importance for evaluation of the portal of entry in patients with septicaemia or infective endocarditis. (c) 2007 The British Infection Society. Published by Elsevier Ltd. All rights reserved.
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页码:204 / 210
页数:7
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